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1.
Int J Gynecol Cancer ; 25(9): 1587-92, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26273932

ABSTRACT

OBJECTIVES: Prognostic risk factors influencing survival in patients with epithelial ovarian cancer (EOC) include tumor stage, grade, histologic subtype, debulking, and platinum status. Little is known about the impact of hormonal milieu and reproductive factors before cancer diagnosis on clinical outcome. We sought to evaluate whether oral contraceptive (OC) use carries any prognostic significance on overall survival (OS) in patients with EOC. METHODS: Newly diagnosed patients with EOC, fallopian tube, and primary peritoneal cancers between 1982 and 1998 were prospectively evaluated with a comprehensive epidemiologic questionnaire. A retrospective chart review was performed to abstract clinicopathologic data, including OS. A Kaplan-Meier analysis was performed to compare survival across various exposures. A Cox regression model was used to compute adjusted hazards ratios (aHRs) and 95% confidence intervals (CIs). RESULTS: We identified 387 newly diagnosed cancers with evaluable information in this cohort. Decreased risk of death was observed in women who reported prior use of OC (aHR, 0.79; 95% CI, 0.58-1.09), previous pregnancy (aHR, 0.77; 95% CI, 0.57-1.04), or a live birth (aHR, 0.81; 95% CI, 0.60-1.08) after adjusting for age at diagnosis, stage, and histologic subtype. Oral contraceptive use was associated with a crude reduced risk of death (HR, 0.55; 95% CI, 0.42-0.72), with reported median OS of 81 months in OC users versus 46 months in nonusers. Patients who reported a single live birth experienced the largest potential survival advantage (aHR, 0.61; 95% CI, 0.39-0.94). Oral contraceptive use and prior pregnancy were associated with improved survival across all strata. CONCLUSIONS: Oral contraceptive use may have lasting effects on epithelial ovarian tumor characteristics conferring favorable prognosis. Putative mechanisms that affect tumor biology include complex interactions between ovarian cells, host immune cells, and hormonal microenvironment during carcinogenesis. Future efforts should be directed to determine the role of reproductive factors in antitumor immunity.


Subject(s)
Contraceptives, Oral/therapeutic use , Fallopian Tube Neoplasms/mortality , Neoplasms, Glandular and Epithelial/mortality , Ovarian Neoplasms/mortality , Peritoneal Neoplasms/mortality , Adolescent , Adult , Aged , Aged, 80 and over , Carcinoma, Ovarian Epithelial , Female , Gravidity , Humans , Kaplan-Meier Estimate , Live Birth , Middle Aged , Parity , Pregnancy , Proportional Hazards Models , Retrospective Studies , Survival Rate , Young Adult
2.
J Low Genit Tract Dis ; 19(3): 189-93, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25856123

ABSTRACT

OBJECTIVE: In this study, we investigated whether regular use of aspirin or acetaminophen was associated with risk of cervical cancer in women treated at an American cancer hospital. METHODS: This case-control study included 328 patients with cervical cancer and 1,312 controls matched on age and decade enrolled. Controls were women suspected of having but not ultimately diagnosed with a neoplasm. Analgesic use was defined as regular (at least once per week for ≥6 months), frequent (≥7 tablets/week), very long term (≥11 years), or frequent, long term (≥7 tablets per week for ≥5 years). RESULTS: Compared to nonusers, frequent aspirin use was associated with decreased odds of cervical cancer (odds ratio, 0.53; 95% confidence interval, 0.29-0.97). A slightly larger association was observed with frequent, long-term use of aspirin (odds ratio, 0.46; 95% confidence interval, 0.22-0.95). Acetaminophen use was not associated with the risk of cervical cancer. CONCLUSIONS: Our findings suggest that frequent and frequent, long-term use of aspirin is associated with decreased odds of cervical cancer. To our knowledge, this is the first US-based study examining these associations. Given the widespread use of nonsteroidal anti-inflammatory drugs and acetaminophen worldwide, further investigations of the possible role of analgesics in cervical cancer, using a larger sample size with better-defined dosing regimens, are warranted.


Subject(s)
Acetaminophen/therapeutic use , Analgesics, Non-Narcotic/therapeutic use , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Aspirin/therapeutic use , Uterine Cervical Neoplasms/prevention & control , Adenocarcinoma/pathology , Adult , Aged , Cancer Care Facilities , Carcinoma, Squamous Cell/pathology , Case-Control Studies , Female , Humans , Logistic Models , Middle Aged , New York , Risk Factors , Surveys and Questionnaires , Uterine Cervical Neoplasms/pathology
3.
Int J Gynecol Cancer ; 25(1): 42-8, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25356535

ABSTRACT

OBJECTIVE: The aim of this study was to determine the tolerability and efficacy of oxaliplatin in patients with recurrent gynecologic malignancies after carboplatin hypersensitivity reactions in comparison with conventionally used cisplatin. METHODS: Forty-six patients were treated with platinum-based chemotherapy from 2006 to 2011 and developed hypersensitivity reactions to carboplatin. Oxaliplatin was administered to 27 patients; 19 patients received cisplatin. Clinicopathologic variables, toxicity, and time-to-failure were analyzed retrospectively using descriptive statistics, Fisher exact, and independent sample permutation t tests. RESULTS: The median number of carboplatin cycles and cumulative dose before reaction were similar in the oxaliplatin and cisplatin groups, respectively (6 vs 7.5 cycles, P = 0.93; 980 [662] mg vs 686 [579.6] mg, P = 0.49). Non-life-threatening hypersensitivity reaction to oxaliplatin developed in 2 of 27 patients. No reactions to cisplatin occurred. The median number of oxaliplatin/cisplatin cycles was 6 in both groups. Complete response to therapy was 34.6% (oxaliplatin) and 31.6% (cisplatin); stable disease was seen in 50.0% and 36.8% of oxaliplatin- and cisplatin-treated patients, respectively (P = 0.46). Exposure to oxaliplatin resulted in less neurotoxicity than cisplatin (25.9% vs 68.4%, P = 0.01). The median number of prior chemotherapy lines in both groups was 2. The median time-to-failure was 10.8 months in oxaliplatin group and 9.8 months in cisplatin group (P = 0.86). CONCLUSIONS: Salvage therapy with oxaliplatin after hypersensitivity reaction to carboplatin is associated with excellent tolerability and time-to-failure comparable to cisplatin. When further administration of carboplatin is precluded, oxaliplatin represents a safe and effective treatment strategy in the platinum-sensitive relapse setting. The significantly lower neurotoxicity profile makes it an attractive alternative to cisplatin.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Drug Hypersensitivity/drug therapy , Genital Neoplasms, Female/drug therapy , Neoplasm Recurrence, Local/drug therapy , Salvage Therapy , Adult , Aged , Aged, 80 and over , Carboplatin/administration & dosage , Cisplatin/administration & dosage , Drug Hypersensitivity/mortality , Drug Hypersensitivity/pathology , Female , Follow-Up Studies , Genital Neoplasms, Female/mortality , Genital Neoplasms, Female/pathology , Humans , Middle Aged , Neoplasm Recurrence, Local/mortality , Neoplasm Recurrence, Local/pathology , Neoplasm Staging , Organoplatinum Compounds/administration & dosage , Oxaliplatin , Prognosis , Remission Induction , Retrospective Studies , Survival Rate
4.
Salud(i)ciencia (Impresa) ; 20(5): 518-520, may.2014.
Article in Spanish | LILACS | ID: lil-790868

ABSTRACT

Los sarcomas ginecológicos con frecuencia auguran un mal pronóstico debido a la diseminación hematógena y por sus metástasis a distancia. Las opciones de tratamiento son limitadas y existen regímenes de quimioterapia que no resultan en una supervivencia prolongada. La resección quirúrgica de las metástasis pulmonares parece ser una medida terapéutica factible en pacientes con recurrencias aisladas, ya que ofrece remisiones prolongadas con una aceptable calidad de vida. En este trabajo se efectuó una revisión de la literatura sobre la supervivencia de las pacientes con sarcomas uterinos y se discute la importancia de los criterios clinicopatológicos que deberían guiar la selección de candidatas óptimas para esta intervención...


Subject(s)
Humans , Gynecology , Sarcoma , Uterus , Lymphatic Metastasis , Ovariectomy , Lung , Drug Therapy , Survivorship
5.
Obstet Gynecol ; 113(2 Pt 2): 557-560, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19155956

ABSTRACT

BACKGROUND: Uterine bleeding frequently complicates gestational trophoblastic disease, particularly after uterine evacuation. Hysterectomy and other procedures used to control this bleeding incur significant risk and can limit fertility. CASE: We present a case of massive hemorrhage complicating uterine curettage performed for metastatic gestational trophoblastic disease. The patient's bleeding was controlled successfully by intrauterine tamponade performed using a balloon catheter. After catheter removal, she achieved complete disease remission. CONCLUSION: Intrauterine balloon catheterization appears to be a promising alternative to control uterine hemorrhage and preserve fertility for young women undergoing treatment for gestational trophoblastic disease. Its use may help avoid invasive interventions, such as hysterectomy and embolization, currently used to control hemorrhage after uterine evacuation.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols , Balloon Occlusion , Catheterization , Dilatation and Curettage/adverse effects , Gestational Trophoblastic Disease/surgery , Lung Neoplasms/secondary , Uterine Hemorrhage/therapy , Adult , Dactinomycin/administration & dosage , Etoposide/administration & dosage , Female , Gestational Trophoblastic Disease/drug therapy , Humans , Leucovorin/administration & dosage , Lung Neoplasms/drug therapy , Methotrexate/administration & dosage , Pregnancy
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